Systems and methods for a de-identified medical and healthcare data marketplace

ABSTRACT

The invention relates generally to systems and methods for a medical data marketplace where de-identified medical data can be offered for sale or licensing, and prospective customers can search for the medical data using various criteria. The marketplace facilitates clinical research activities, clinical trials, medical research, medical technology development, and the like, while preserving HIPAA privacy protections, and allows medical data owners to monetize the data in an efficient manner.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims the benefit of U.S. Non-Provisional patentapplication Ser. No. 17/029,221 entitled “SYSTEMS AND METHODS FORDE-IDENTIFYING MEDICAL AND HEALTHCARE DATE” filed on Sep. 23, 2020,which claims priority to U.S. Non-Provisional patent application Ser.No. 16/674,120 entitled “SYSTEMS AND METHODS FOR DE-IDENTIFYING MEDICALAND HEALTHCARE DATA” filed on Nov. 5, 2019, which claims priority toU.S. Provisional Patent Application No. 62/756,132 entitled “SYSTEM ANDMETHOD FOR DE-IDENTIFYING DATA” filed on Nov. 6, 2018, all of which arecommonly owned and incorporated herein by reference in their entireties.

BACKGROUND Field of the Invention

The present invention relates, in general, to systems and methods forprotecting patient privacy when health care and medical information isshared between various entities and, in particular, to systems andmethods that implement a multi-stage sanitizing routine forde-identifying protected health information (PHI) from medical andhealthcare data, such as, for example, medical reports and diagnosticimages, in order to ensure patient privacy, while preserving the abilityfor sanitized medical reports and diagnostic images to be re-identified.

Description of Related Art

The ease with which electronic data can be transmitted, together withthe increasing use of health care, medical, and patient information(collectively, “medical information”) for research purposes, has raisedconcerns about patient confidentiality and institutional liability, aswell as concerns surrounding the protection of patient privacy when suchmedical information is transmitted between various entities, such as,for example, a medical provider and a research institution.

To maintain patient privacy in the context of research and variousthird-party uses, it must be ensured that any medical information usedin aggregate is not associated with any specific patient or individual,and that only authorized entities based on a patient's informed consenthave access to such medical data.

Such patient privacy can be maintained by disclosing only specificportions of the medical information through de-identification processes,where portions of the medical information that may be classified aspersonally identifiable information (PII). PII can be any data thatcould potentially identify a specific patient or individual. SensitivePII is information which, when disclosed, could result in harm to anindividual whose privacy has been breached. Sensitive PII can includebiometric information, medical information, personally identifiablefinancial information, and unique identifiers such as passport or SocialSecurity numbers. PHI and PII is typically removed, deleted, masked, orreplaced with non-identifiable information through such conventionalde-identification processes.

In the United States, standards such as Health Insurance Portability andAccountability Act (HIPAA) have resulted in federal regulations thatplace strict requirements on the archiving and disclosure of medicalinformation. For example, in accordance with HIPAA, federal regulationshave been enacted that require healthcare organizations, physicians, andentities having access to such medical information to ensure theprotection, privacy and security of the patient information, which caninclude PHI and PII. In particular, the “Privacy Rule” of HIPAA providesfederal privacy regulations that set forth requirements forconfidentiality and privacy policies and procedures, consents,authorizations and notices, which must be adopted in order to maintain,use, or disclose PHI and PII in the course of a patient's treatment, aswell as other business functions or other activities.

The HIPAA Privacy Rule allows for entities to de-identify PHI forcertain purposes so that medical information may be used and disclosedfreely, without being subject to the protections afforded by the PrivacyRule. The term “de-identified data” as used by HIPAA refers to medicalinformation from which all information, data and tags that couldreasonably be used to identify the patient has been removed (such as,for example, their name, address, social security number, date of birth,contact information, and the like).

Conventional methods for de-identifying medical data include simplystripping all information considered to be PHI or PII from a medicalrecord that can be used to determine the identity of a patient, orreplacing such information with something else (such as, for example,replacing the actual patient name with the string “name”). Although themedical records are de-identified with such conventional methods, thereremains no mechanism by which PHI or PII can be recovered forre-identification purposes, if required.

In addition, various methods of de-identification generally of documentsand metadata fields include built-in code to remove portions marked forde-identification, or utilize template-based approaches to redactinformation from documents. Methods of de-identification have been usedfor text documents, structured metadata fields such as in DigitalImaging and Communications in Medicine (DICOM) metadata, butde-identification of visual media data when the medical information isburned into, or embedded inside the media, can be difficult and timeconsuming.

Therefore, there is a need for a reliable system and method to ensurecomplete de-sanitization of both diagnostic images and associatedmedical reports containing text and burned in medical information,whereby the sanitized PHI and PII can be recovered for re-identificationpurposes.

SUMMARY

In one embodiment, the invention relates to a system for providing amedical data marketplace, the system comprising: a database storing aplurality of de-identified medical data sets, wherein each de-identifiedmedical data set is owned by a different data owner; a server coupled tothe database; and a computer-readable storage medium operably connectedto a processor coupled to the server, the computer-readable storagemedium containing programming instructions that, when executed, causethe processor to: generate an interface that allows a customer to submita search request that includes at least one criteria, receive the searchrequest from the interface, query the database using the criteria toretrieve at least one matching medical data set from the plurality ofde-identified medical data sets, display the at least one matchingmedical data set on the interface, and facilitate a financialtransaction related to the at least one matching medical data setbetween a respective data owner and the customer.

In another embodiment, the invention relates to a system for providing amedical data marketplace, the system comprising: a database storing aplurality of diagnostic image sets, wherein each diagnostic image set isowned by a different data owner; a server coupled to the database; and acomputer-readable storage medium operably connected to a processorcoupled to the server, the computer-readable storage medium containingprogramming instructions that, when executed, cause the processor to:perform a de-identification process on each of the plurality ofdiagnostic image sets to generate a plurality of de-identifieddiagnostic image sets, generate an interface that allows a customer tosubmit a search request that includes at least one criteria, receive thesearch request from the interface, query the database using the criteriato retrieve at least one matching diagnostic image set from theplurality of de-identified diagnostic image sets, display the at leastone matching diagnostic image set on the interface, and facilitate afinancial transaction related to the at least one matching diagnosticimage set between a respective data owner and the customer.

In another embodiment, the invention relates to a system for providing amedical data marketplace, the system comprising: a database storing aplurality of medical data sets, wherein each medical data set is ownedby a different data owner; a server coupled to the database; and acomputer-readable storage medium operably connected to a processorcoupled to the server, the computer-readable storage medium containingprogramming instructions that, when executed, cause the processor to:perform a de-identification process on each of the plurality of medicaldata sets to generate a plurality of de-identified medical data sets,generate an interface that allows a customer to submit a search requestthat includes at least one criteria; receive the search request from theinterface, query the database using the criteria to retrieve at leastone matching medical data set from the plurality of de-identifiedmedical data sets, display the at least one matching medical data set onthe interface, and facilitate a financial transaction related to the atleast one matching medical data set between a respective data owner andthe customer.

BRIEF DESCRIPTION OF THE DRAWINGS

These and other embodiments of the disclosure will be discussed withreference to the following exemplary and non-limiting illustrations, inwhich like elements are numbered similarly, and where:

FIG. 1 is a network architecture diagram of a system for de-identifyingmedical data, according to an embodiment of the invention;

FIG. 2 is a flowchart illustrating the steps of selecting medical datafor de-identification, according to an embodiment of the invention;

FIG. 3 is a flowchart illustrating the steps of de-identifying DICOMmetadata and medical reports, according to an embodiment of theinvention;

FIG. 4 is a flowchart illustrating the steps of creating ade-identification profile for a diagnostic modality, according to anembodiment of the invention;

FIG. 5 is a flowchart illustrating the steps of de-identifying burned inPHI on diagnostic images, according to an embodiment of the invention;

FIG. 6A is view of a diagnostic image prior to being de-identified,according to an embodiment of the invention;

FIG. 6B is a view of a diagnostic image after being de-identified,according to an embodiment of the invention;

FIG. 7A is a view of a dialogue window with a selection tool used toselect PHI regions to create a de-identification profile, according toan embodiment of the invention;

FIG. 7B is a view of a dialogue window with a selection tool used toselect non-PHI regions to create a de-identification profile, accordingto an embodiment of the invention;

FIG. 8 is a view of a region of interest identified by image analysis,according to an embodiment of the invention;

FIG. 9 is a table with exemplary DICOM metadata, according to anembodiment of the invention; and

FIG. 10 is a flowchart illustrating the steps of re-identifying medicaldata, according to an embodiment of the invention.

DEFINITIONS

The following definitions are meant to aid in the description andunderstanding of the defined terms in the context of the presentinvention. The definitions are not meant to limit these terms to lessthan is described throughout this application. Such definitions aremeant to encompass grammatical equivalents.

As used herein, the term “medical data” can refer to, for example,health and healthcare related data, patient data, electronic medicalrecords, medical imaging studies, medical and diagnostic images,diagnostic reports, fitness and activity data, medical reports, and thelike.

As used herein, the term “medical reports” can refer to, for example,any patient data, patient charts, diagnostic notes, opinions, reads andreports, medical test and laboratory results, surgical history, familyhistory, medications, medical allergies, social history, habits (suchas, for example, drug, tobacco and alcohol use), immunization history,clinical information, growth and development history, medicalencounters, physical examination observations, progress notes, and thelike.

As used herein, the term “recipient” can refer to, for example, medicalclinics, hospitals, medical providers, health insurance providers,diagnostic sites, imaging sites, data customers, and the like. A“recipient” can further refer to entity or individual that analyzes,processes, compiles, or otherwise utilizes aggregate medical andhealth-related data for research, analytics, advertising, marketing,monetization, or reporting purposes. The recipient can be an academicinstitution, a government research laboratory, a non-profit entity, or afor-profit entity, such as a pharmaceutical, health insurance,biotechnology, wearable device, physiological monitoring, or medicaldevice company.

As used herein, the term “PHI” can refer not only protected healthinformation, but also to PII and any other information that may beconsider private, confidential, personally identifying, financialinformation, and the like.

DETAILED DESCRIPTION

It should be understood that aspects of the invention are describedherein with reference to the figures, which show illustrativeembodiments. The illustrative embodiments herein are not necessarilyintended to show all embodiments in accordance with the invention, butrather are used to describe a few illustrative embodiments. Thus,aspects of the invention are not intended to be construed narrowly inview of the illustrative embodiments. In addition, although theinvention is described with respect to its application for the transferof medical information containing DICOM data applications, it isunderstood that the system could be implemented in any setting where thetransfer of any type or form of medical or patient data may be useful.

FIG. 1 is a network architecture diagram of a system for de-identifyingmedical data, according to an embodiment to the invention. The systemincludes a data provider 100 that is communicatively coupled to aninstitution 106, such as a medical facility, hospital, health careprovider, diagnostic imaging center, diagnostic imaging station, and thelike. In an embodiment, the institution 106 can include a picturearchiving and communication system (PACS) 108 via a communication link109. The data provider 100 can be remote from the PACS 108, and the dataprovider 100 can be communicatively coupled to multiple local ordistributed PACS (not shown).

In an embodiment, the data provider 100 is operated by a third-party notaffiliated with, or owned or operated by, the institution 106. The dataprovider 100 facilitates the transfer of de-identified medical databetween the PACS 108 and various third-party recipients 112. The dataprovider 100 can facilitate an encrypted direct peer-to-peercommunication channel for securely transferring medical data between thePACS 108 and/or database 102 and such third-party recipients 112, wherethe PACS 108 and/or database 102 are not within a data transfer networkutilized by a recipient 112. The encrypted direct peer-to-peercommunication channel is described in more detail in commonly ownedapplication Ser. No. 16/281,409, entitled, METHODS AND SYSTEMS FORTRANSFERRING SECURE DATA AND FACILITATING NEW CLIENT ACQUISITIONS, thecontents of which are hereby incorporated by reference in its entirety.

In an embodiment, the data provider 100 can include computing hardwareand software, such as a database 102 and sanitizing engine 104. Inanother embodiment, the database 102 and/or sanitizing engine 104 can becloud-based, and located remotely from the data provider 100, such as ona remote server provided by Amazon Web Services® or the like. In anembodiment, the data provider 100 is configured as a server, virtualserver, or a distributed server can store data, as well as executeprograms, algorithms, scripts, and applications.

The data provider 100 is communicatively coupled to a network 110 via acommunication link 111, where the network 110 in turn is communicativelycoupled to a recipient 112 via communication link 113.

In an embodiment, the recipient 112 can be a customer that purchasesde-identified medical data. The recipient 112 can purchase de-identifiedmedical data in bulk, with specific criteria, or in bulk. The cost ofsuch de-identified medical data can be based on the number of medicaldata requested, the modality of medical data requested, the extent ofsanitizing required, and/or custom sanitizing requirements.

In an embodiment, the recipient 112 can also include a database 114, anda virtual machine 116, where the virtual machine 116 is a softwareinstance that is operated, provided, or developed by the data provider.

As described herein the, databases 102 and 114 can be centralized andstored on respective servers, or can be distributed databases. In anembodiment, the databases 102 and 114 can be relational databases, orcan leverage blockchain technology.

The communication links 109, 111 and 113 may be any type ofcommunication links suitable to allow interaction between the dataprovider 100 and PACS 108, the data provider 100 and recipient 112, aswell as with the network 110. For example, the communication links 109,111 and 113 may each be a wired network, a wireless network, or anycombination thereof. Further, communication links 109, 111 and 113 mayinclude a distributed computing network, an intranet, a local-areanetwork (LAN) and/or a wide-area network (WAN), or any combinationthereof. For example, the LAN may make use of WIFI in its manyvariations and the WAN may make use of broadband, cellular and/orsatellite networks using technologies including, but not limited to,CDPD, CDMA, GSM, PDC, PHS, TDMA, FLEX, ReFLEX, iDEN, TETRA, DECT,DataTAC, Mobitex, EDGE and other 2G, 3G, 4G and LTE technologies.However, those of ordinary skill in the art will appreciate that thecommunication links 109, 111 and 113 are not limited thereto. In anotherembodiment, the communication links 109, 111 and 113 may each includeethernet, Firewire, parallel, serial, or USB connections, or short-rangecommunication protocols such as Bluetooth, infrared, Zigbee, and thelike.

In an embodiment, a medical data marketplace 118 can be communicativelycoupled to the network 110. The medical data marketplace 118 can allowsellers, such as data providers, institutions, medical serviceproviders, hospitals, medical clinics, and/or individual patients tooffer de-identified medical data for sale or license to variousthird-party customers.

In an embodiment, the medical data marketplace 118 can allow customersto search for, and purchase, medical data based on specific criteria.The criteria can include, for example, modality type, equipmentmanufacturer, body part, a study description, protocol name, a requestedprocedure description, a scheduled procedure step description, and/or akeyword or Boolean search. In an embodiment, the query can include oneor more criteria, and can further include a study date or study daterange. The criteria can further include a geographic criteria, such as atown, city, state, country, or geographic region, as well as ademographic criteria, such as a patient race, a patient age, and patientsex. In an embodiment, customers can further search for medical databased on a defined metadata tag.

In an embodiment, customers may also purchase medical data in bulk, suchas random lots, or lots matching at least one criteria. In anembodiment, the data provider 100 can operate, own, or manage themedical data marketplace 118, and the data provider 100 can receive acommission from each medical data transaction that occurs on the medicaldata marketplace 118, with the seller also receiving a portion of theproceeds from the transaction with the customer. In addition, the dataprovider 100 can also receive a listing fee from sellers, as well as amembership fee from customers.

In another embodiment, the medical data marketplace 118 can offerauctions on medical data. The medical data marketplace 118 can furtherutilize blockchain technology to provide anonymity, privacy, andsecurity for both sellers and customers.

In yet another embodiment, each of the sellers participating on themedical data marketplace 118 can collectively or cooperatively share theproceeds that are generated from transactions on the medical datamarketplace 118. In an embodiment, each seller can receive an equalamount of the proceeds. In another embodiment, each seller can receive apro-rata amount of the proceeds based on the percentage of datacontributed by each seller relative to the total amount of data on themarketplace.

FIG. 2 is a flowchart illustrating the steps of selecting medical datafor de-identification, according to an embodiment of the invention. Inan embodiment, at step 200, a user can access a portal, such as a secureweb site via a Uniform Resource Location (URL) using a browser on acomputing device. The portal can be stored on or executed from, forexample, the data provider 100, and the portal allows the user toretrieve medical data stored on the database 102.

In an embodiment, prior to being able to access the portal, the usermust enter credentials, such as a login and password, or other indiciathat verifies their identity. The credentials can include user's mobiledevice number, login, password, email address, phone number, accountnumber, personal identification number (PIN), name, driver's licensenumber, social security number, birthdate, employee number, and/or aunique account identification code previously provided to the user by anauthorizing entity, such as an employer or data provider. In anotherembodiment, the credentials can be biometric, such as a fingerprint,iris, facial, or voice scan. In yet another embodiment, the credentialcan be a gesture input by the user, such as a on a touchscreen ortouchpad.

In an embodiment, the user is external to, and not affiliated with, thedata provider 100, but rather affiliated with the recipient 112. Therecipient 112 and the data provider 100 can have a business arrangementor contractual agreement in place that allows the user to access thedatabase 102 via the portal. In this embodiment, the user may access theportal via the virtual machine 116 located at the recipient 112 which iscommunicatively coupled to the data provider 100.

In another embodiment, the user can access the portal directly via theirPACS, such as PACS 108 or a PACS located at, or operated by, therecipient 112.

At step 202, the user can enter a query by selecting from variouscriteria, such as, for example, modality type, equipment manufacturer,body part, a study description, protocol name, a requested proceduredescription, a scheduled procedure step description, and/or a keyword orBoolean search. In an embodiment, the query can include one or morecriteria, and can further include a study date or study date range. Thequery can further include a geographic criteria, such as a town, city,state, country, or geographic region, as well as a demographic criteria,such as a patient race, a patient age, and patient sex. In anembodiment, the user can perform a query based on a defined metadatatag.

In another embodiment, the query can include a medical condition orailment, such as, for example, brain tumors, cancers, traumatic braininjury, developmental anomalies, multiple sclerosis, stroke, dementia,infection, fractures, bone bruises, etc.

At step 204, the query results are displayed to the user. The queryresults can be matching medical data that are returned to the user,where the medical data information displayed does not include any PHI.For example, the user may only be shown the patient age, sex, andcriteria that matches the query from each matching medical data. In thisembodiment, the medical data are not yet sanitized; however, the usermay only view non-PHI details in order to select medical data forde-identification. In an embodiment, the data provider 100 utilizesStructured Query Language (SQL) to retrieve the query results from thedatabase 102. In another embodiment, the data provider 100 can utilizevarious relational alternatives to SQL, as well as alternatives thatutilize search frameworks for non-relational database models.

At step 206, the user can select the desired medical data tode-identify. In an embodiment, the medical data consists of diagnosticstudies which include diagnostic images, such as radiology images, aswell as diagnostic reads, interpretation, clinical information, notes orreports related to those diagnostic images.

The user can manually select individual medical data to de-identify, orcan select all medical data in the query results. In another embodiment,the user can filter the query results to obtain a narrower result set.For example, if the user initially queried for all medical data for“males” and “brain tumor”, the user can filter the results further by,for example, an age range, a geographic filter, a modality type, and thelike. The user can then automatically select medical data to de-identifybased on the results of a subsequent filtering operation, for example,such as all medical data from a male patient, or all medical data frompatients under the age of 60, etc.

At step 208, the user can select a destination to store or transmit thede-identified medical data to. In an embodiment, if the user is externalto the data provider 100, then the destination can only be affiliatedwith the recipient 112. If the user is internal to the data provider100, or institution 106 being serviced by the data provider 100, thenthe user can select a specific internal or external destination.

In another embodiment, the de-identified medical data can beautomatically routed to a pre-specified or pre-determined destination.For example, the de-identified medical data can be routed based onpre-defined routing rules, a pre-defined destination based on the user'sprofile, a pre-defined destination based on the recipient 112, or basedon a previously utilized destination by the user.

In another embodiment, the pre-defined destination can be determined bythe institution 106 or the data provider 100. For example, theinstitution 106 or the data provider 100 may only allow certaindestinations to receive de-sanitized medical data, and the user may belimited to selecting from a pre-defined list of destinations, or may belimited to an automatically selected destination whereby the user doesnot have the ability to modify, select, or change the destination.

FIG. 3 is a flowchart illustrating the steps of de-identifying DICOMmetadata and medical reports, according to an embodiment of theinvention. At step 300, the data provider 100 and/or the sanitizingengine 104 receives the request to de-identify the medical data selectedby the user at step 206. The selected medical data are imported into thesanitizing engine 104 from the database 102. At step 302, the sanitizingengine 104 determines if a selected medical data has previously beende-identified. If the selected medical data has previously beende-identified, then at step 304, the de-identified medical data isretrieved from the database 102, or from another databasecommunicatively coupled to the data provider 100, and the de-identifiedmedical record is transmitted to the destination specified at step 208.

In an embodiment, the destination is a network or electronic address forthe virtual machine 116, where the virtual machine 116 is configured toreceive the de-identified medical data.

If the selected medical data has not been previously de-identified, thenat step 306, the sanitizing engine 104 determines if associated medicalreports are stored with the diagnostic images in the medical data, suchas images obtained via medical imaging modalities such as digital X-ray,Computed Tomography (CT), computed radiography, Magnetic ResonanceImaging (MM), Positron Emission Tomography (PET), thermoacousticimaging, film-based optical imaging, ultrasound imaging, and nuclearmedicine-based imaging.

In an embodiment, the diagnostic images can be DICOM encapsulated filesthat contain a document, such as a PDF document, that have beenencapsulated with a DICOM information object and/or DICOM image(s).

If associated medical reports are not stored with diagnostic imageswithin the medical data, then at step 308, the data provider 100retrieves the associated medical reports from a corresponding storagelocation. In an embodiment, the corresponding storage location can be adatabase on the data provider 100, such as database 102, or can belocated on the PACS 108, another server, distributed server system, datastorage facility, or provided by another data provider.

At step 310, the sanitizing engine 104 extracts content from theassociated medical reports, and packages the extracted content asmedical report text. The process then continues to step 312, as isdescribed in more detail below.

If the sanitizing engine 104 determines that associated medical reportsare stored with the diagnostic images in step 306, then the processcontinues to step 312 where header data and image data are extractedfrom the DICOM encapsulated file. In an embodiment, the sanitizingengine 104 extracts the DICOM image into a JPEG image, and extracts theheader data into a parseable document, such as a document in an XML,JSON, YAML, AXON, ConfigObj, OGDL, HDF, SSYN, SDL, Boulder, ONX, SMEL,GroovyMarkup, ATerms, LNML, GODDAG, JITTs, UBF format, and the like.

At step 314, the header data and the parseable document are copied andstored into a database 114, such as database 114 affiliated withrecipient 112. In an embodiment, the header data and the parseabledocument can be stored with the addition of a private tag fieldcontaining a randomly generated key to be used for re-identificationpurposes. However, the private tag field may not be mandatory. In anembodiment, the randomly generated key is not used to decrypt thedatabase 114. In an embodiment, the database 114 can be encrypted, oralternatively, the header data and the parseable document are stored inan encrypted fashion. In an embodiment, step 314 is an optional step,and executed only if the data provider 100 or institution 106 hasenabled, requested, or allowed for re-identification of the medicaldata. In an embodiment, the header data and/or parseable document isassociated with a unique identification string, such as a number,characters, alpha-numeric sequence, and the like, when stored into thedatabase 114, where the unique identification string is used forre-identification.

In an embodiment, the unique identification string is a SOP instanceunique identification (SOP instance UID). In an embodiment, the uniqueidentification string is generated using a hexadecimal salt hashingmechanism, such that the unique identification string has no relation tothe underlying patient, patient data, PHI, PII, or information thatexisted in the header data, parseable document, or medical data prior tothe de-identification process.

In an embodiment, the unique identification string is stored in adedicated database, such as database 114 maintained by the recipient112. In another embodiment, the unique identification string is storedin a dedicated database that is maintained by the institution 106, thedata provider 100, the recipient 112, or a covered entity that isassociated with the user, and which is configured to receive thede-identified medical data. In another embodiment, the dedicateddatabase can be local to the user, the recipient 112, or the institution106, can be located on the data provider 100, or can be located onanother server, distributed server system, or data storage facility.

At step 316, the parseable document is parsed for DICOM metadata. In anembodiment, the DICOM metadata, such as DICOM tags, can be selected forthe purposes of de-identification so that the de-identification complieswith § 161.514(b)(2) and § 161.514(c) of the HIPAA Privacy Rule. FIG. 10described herein is an exemplary list of DICOM metadata that may beutilized for de-identification. In another embodiment, the user,recipient 112, data provider 100, and/or institution 106 can configurethe specific tags to be sanitized by the de-identification process.

At step 318, the DICOM metadata are sanitized by the sanitizing engine104. In an embodiment, the sanitizing engine 104 fills the DICOMmetadata fields with randomly generated characters. The sanitizingengine 104 utilizes an algorithm or script to generate the randomcharacters such that the random characters have no relation to theunderlying patient, patient data, PHI, PII, or information that existedin the header data or medical data prior to the de-identificationprocess.

In another embodiment, the DICOM metadata fields are cleared so thatthey are empty, or they are blacked out with a black shape, such as apolygon, rectangle, circle, square, free-form, and the like.

In yet another embodiment, the sanitizing engine 104 utilizes analgorithm or script to generate a specific string of replacementcharacters. For example, if a recipient, such as a customer, can providespecific instructions of how information in DICOM metadata should bereplaced or restructured. For example, a recipient 112 may request thatthe “patient ID” metadata field is replaced with a string in a certainformat based on where the medical data originated. In an illustrative,non-limiting example, the first three digits of the original “patientID” is replaced with “001” to indicate a first provider, or replacedwith “002” to indicate a second provider.

Thus, a recipient 112 can provide instructions or a template on howcertain or all DICOM metadata fields should be replaced, restructured,and/or appended. In an embodiment, a recipient 112 can create differenttemplates based on diagnostic modalities, imaging locations, imagingequipment, imaging procedures, and the like.

At step 320, the medical report text is analyzed to identify instance ofPHI, and the identified PHI is sanitized by the sanitizing engine 104.In an embodiment, the sanitizing engine 104 replaces the PHI in themedical report text with randomly generated characters. The sanitizingengine 104 utilizes an algorithm or script to generate the randomcharacters such that the random characters have no relation to theunderlying patient, patient data, or information that existed in theheader data or medical data prior to the de-identification process. Inan embodiment, the sanitizing engine 104 may utilize natural languageprocessing to identify instances of PHI.

Furthermore, the sanitizing engine 104 can use regular expressionmechanisms (also known as RegEx, RegExp, or R.E.) to identify andsanitize characters and text. For example, regular expression can beused to identify and sanitize initials, geographic location coordinates,text fragments, and the like.

In another embodiment, the sanitizing engine 104 can analyze sanitizedmedical reports over time using machine learning to more efficiently andquickly identify instances of PHI on future medical reports.

In another embodiment, the PHI is cleared so that the underlying fieldwhere the PHI is located is empty, or the PHI is blacked out with blackrectangles.

FIG. 4 is a flowchart illustrating the steps of creating ade-identification profile for a diagnostic modality, according to anembodiment of the invention. In an embodiment, pre-definedde-identification profiles can be generated for different diagnosticmodalities, imaging locations, imaging equipment, imaging procedures,and the like. The de-identification profiles allow known, standard, orcommon areas that contain PHI on a diagnostic image to be defined for aspecific diagnostic modality, such that a blackout zone or sanitizingprocess can be applied to such areas on any diagnostic image thatmatches the de-identification profile (i.e., any diagnostic image that,for example, is generated using the specific modality that thede-identification profile was created for).

At step 400, the data provider 100 determines if the user has permissionto create a de-identification profile for a diagnostic modality. In anembodiment, only authorized users can create a de-identificationprofile, and the authorization is designated by an administratoraffiliated with the data provider 100 or institution 106. If the userdoes not have permission, the process continues to step 402, where theuser is prompted to obtain authorization.

If, however, the user has permission to create a de-identificationprofile, then at step 404, a dialogue window is displayed to the user,where the dialogue window includes a diagnostic image from one of theselected medical data. At step 406, the user is prompted to selectportions of the diagnostic image containing PHI using a selection tool.The selection tool can take various shapes, and in an embodiment, can bea rectangular selection tool.

In other embodiments, the selection tool can be free form, or takevarious shapes such as elliptical, circular, column, row, square, alasso and the like. In another embodiment, the selection tool can be amagnetic lasso tool which follows lines and outlines like a magnet, andfacilitates the selection of PHI areas having contours.

In an embodiment, the user can manipulate the size and dimensions of theselection tool, so that a larger or smaller area of the diagnostic imagecan be selected.

In an embodiment, the selection tool can further be a magic wand toolwhich facilitates the selection of a specific color in an area withcontrasting colors. For example, the magic wand tool allows for anentire PHI area which may have a white background to be selected wherethe remaining non-PHI areas of the diagnostic image are black.Similarly, the selection tool can have an inverse feature where theinverse color is automatically selected. For example, the inversefeature allows for all non-black areas to be selected by the user.

At step 408, all selected portions are sanitized from the diagnosticimage, such as by masking with a blackout zone, in order to generate apreview of the sanitized diagnostic image for the user. In anotherembodiment, the selected portions are deleted, blurred, obfuscated,cropped, or otherwise made illegible. In yet another embodiment, anypixels, characters, or text in the selected portions are replaced withrandomly generated characters. In this embodiment, the sanitizing engine104 utilizes an algorithm or script to generate the random characterssuch that the random characters have no relation to the underlyingpatient, patient data, medical data, or information that existed on thediagnostic image prior to the de-identification process.

In another embodiment, the user can be prompted at step 406 to selectportions of the diagnostic image that do not contain PHI. In thisembodiment, at step 408, all non-selected portions are sanitized fromthe diagnostic image in order to generate a preview of the sanitizeddiagnostic image for the user.

At step 410, once the diagnostic image has been sanitized, the user canbe prompted to confirm that no additional PHI remains visible on thediagnostic image. If PHI remains visible, the process returns to step406 where the user can again select areas with PHI to be sanitized.

If no PHI remains visible, then the process continues to step 412 wherethe de-identification profile is saved to the data provider 100 orvirtual machine 116 for subsequent retrieval when a medical datamatching the de-identification profile is selected for sanitizing.

In an embodiment, the modality information, equipment manufacturer,station information, and respective location information is saved to thedata provider 100 or virtual machine 116. In addition, the dimensions ofthe diagnostic image used to generate the de-identification profile isstored so the data provider 100 can determine if future images to-besanitized are appropriate candidates for the de-identification profile.For example, the dimensions can include the size (in, for example,pixels, inches, centimeters, etc.) of the diagnostic image, an aspectratio of the diagnostic image, and/or a resolution of the diagnosticimage. In another embodiments, properties such as the quality,compression, amount of loss, and the like, can also be stored.

In yet another embodiment, the de-identification profile can beautomatically generated, using for example, machine learning. Forexample, previously generated de-identification profiles can be analyzedbased on accuracy over time, in order to generate futurede-identification profiles based on historical sanitization success orfailure results.

FIG. 5 is a flowchart illustrating the steps of de-identifying burned inPHI on diagnostic images, according to an embodiment of the invention.At step 500, the data provider 100 determines is a de-identificationprofile exists for a modality that produced a diagnostic image within aselected medical data. In an embodiment, the data provider 100 comparesvarious DICOM metadata contained in the diagnostic image, such as, forexample, the modality, equipment manufacturer, station information, andother station or equipment-based tags, or pre-defined user tags.

If the DICOM metadata on the diagnostic image do not match an existingde-identification profile, then the user is promoted to create ade-identification profile at step 502, and the process returns to step400 as shown in FIG. 4.

If, however, the DICOM metadata on the diagnostic image match anexisting de-identification profile, then the process continues to step504 where the size of the diagnostic image is compared to the image sizespecified in the de-identification profile. In an embodiment, insteadof, or in addition to the comparison of size, the properties of thediagnostic image, such as its aspect ratio, resolution, quality, amountof loss, and the like can compared against the properties stored in thede-identification profile.

In an embodiment, the comparison can be based on a threshold value,where the sanitizing engine 104 determines if a selected diagnosticimage is within a certain threshold of the size or properties of thede-identification profile. The threshold value can be manuallydetermined, or can be determined by the data provider 100 or sanitizingengine 104 over time using machine learning, based on analysis of priorsanitizing results using de-identification profiles.

If, however, the diagnostic image does not match, or is not within anacceptable threshold value of, the size and/or properties in thede-identification profile, then the process continues to step 506 wherethe diagnostic image is held in a queue for manual review. In anembodiment, the process can return to step 400 as shown in FIG. 4, wherethe user is prompted to create a new de-identification profile.

If the diagnostic image matches, or is within an acceptable thresholdvalue of, the size and/or properties in the de-identification profile,then at step 508, blackout zones are automatically applied to thediagnostic image at the area(s) specified in the de-identificationprofile. In another embodiment, the area(s) specified in thede-identification profile are deleted, blurred, obfuscated, cropped, orotherwise made illegible instead of, or in addition to, being appliedwith a blackout zone.

In another embodiment, if there are multiple areas of a diagnostic imagespecified in the de-identification profile to be sanitized, the user canbe prompted to review each area prior to the processing by thesanitizing engine 104. For example, the user can approve or reject asanitizing operation of an area specified in the de-identificationprofile based on if there is actual PHI present on a specific diagnosticimage, or if a diagnostic portion of the image is located in thespecified area(s).

Next, at step 510, a first stage of quality control is performed by thesanitizing engine 104 where optical character recognition (OCR) isperformed on a portion of, or the entire, diagnostic image, after theblackout zones have been applied. At step 512, the sanitizing engine 104analyzes the diagnostic image after the OCR process to determine if anytext or characters remain on the diagnostic image.

In an embodiment, the sanitizing engine 104 only analyzes the areasspecified in the de-identification profile that contain PHI to determineif any pixels, text or characters (collectively, “pixels”) still remain.If pixels are identified in these areas, then the sanitizing operationperformed in step 508 is deemed to have failed. In this embodiment, theOCR operation is only be performed on the area specified in thede-identification profile, and where the blackout zone or sanitizingprocess has been applied, and not on the entire diagnostic image.

In another embodiment, the sanitizing engine 104 analyzes the entirediagnostic image, and not only the areas specified in thede-identification profile. In this embodiment, the OCR operation can beperformed on the entire diagnostic image, and is not limited to anyareas of the diagnostic image, or just where the blackout zone orsanitizing process has been applied.

If any pixels are identified in the diagnostic image after the OCRoperation, then the process continues back to step 506, where thediagnostic image is held in a queue for manual review. The user can beprompted to review the diagnostic image and compare it to thede-identification profile to determine if the any aspect of thediagnostic modality that created that specific diagnostic image may havechanged, resulting in the de-identification profile to no longer beaccurate or applicable.

If, however, no pixels are identified in the diagnostic image after theOCR operation, then at step 514, a second stage of quality control isperformed by the sanitizing engine 104 using an image analysistechnique. In an embodiment, the image analysis is used to detect agradient boundary (i.e., a directional change in the intensity or colorin an image) on the diagnostic image in order to determine where theactual diagnostic portion of the image ends. The diagnostic portion canbe referred to the region of interest in the diagnostic image, and thegradient boundary identifies the bounds of the region of interest. Step514 is an optional step, and is not mandatory.

At step 516, the sanitizing engine 104 determines if any white ornon-black pixels exist outside of the region of interest. If any whiteor non-black pixels are identified outside of the region of interest,then at step 518, these pixels are converted, masked, or turned black bythe sanitizing engine 104. In another embodiment, these pixels aredeleted, blurred, obfuscated, cropped, or otherwise made illegible. Theprocess then returns to step 510, where an OCR operation is performed onthe diagnostic image again. Step 516 is an optional step, and is notmandatory.

If, however, no white or non-black pixels are identified outside of theregion of interest, then at step 520, the sanitized parseable documentand sanitized JPEG image are re-encapsulated back into the DICOM formatby the data provider 100 or the sanitizing engine 104. The DICOMre-encapsulated file is now sanitized of any PHI, and is ready to betransmitted to third-party recipients at step 522. The third-partyrecipients can be internal or external to the data provider 100, orinstitution being serviced by the data provider 100.

FIG. 6A is view of a diagnostic image prior to being de-identified,according to an embodiment of the invention. The diagnostic image 600includes a diagnostic portion 602, also referred to as the region ofinterest, as well as non-PHI areas 604 and PHI area 606. FIG. 6A is anexemplary diagnostic image 600, and the invention is not limited to anyspecific modality, and the diagnostic image can include multiple PHIareas at various other locations on the diagnostic image, as well asmultiple non-PHI areas at various other locations on the diagnosticimage.

In an embodiment, the PHI area 606 includes personally identifiableinformation, such as a patient's name, date of birth, social securitynumber, accession numbers, and medical record number. In addition, thePHI area can further include location and site information, such as theinstitution name, referring physician name, and the like.

In an embodiment, the non-PHI areas 604 include equipment, modality,scan, and/or image specific information, such as the type ofscan/modality, image dimensions, slice thickness, echo time, the numberof phase encoding steps, repetition time, body part, equipmentmanufacturer, and the like.

FIG. 6B is a view of a diagnostic image after being de-identified,according to an embodiment of the invention. As shown in FIG. 6B, PHIarea 606 is blacked out with a blackout zone, such that the PHI shown inFIG. 6A is no longer visible. However, the non-PHI areas 604 remainvisible to the user.

FIG. 7A is a view of a dialogue window with a selection tool used toselect PHI areas to create a de-identification profile, according to anembodiment of the invention. In an embodiment, the user utilizes aselection tool 700 to select areas of the diagnostic image 600 thatcontains PHI, after the diagnostic image has undergone an OCR process,as described above. The selection too 700 can be operated by an inputdevice such as a mouse, trackball, touchpad, pointing stick, or atouchscreen. In another embodiment, the user can manipulate theselection tool 700 using gestures either via touching a touchscreen, orwhich are transmitted via a user's wearable device to the user'scomputing device on which the dialogue window is displayed.

In an embodiment, the selection tool 700 is used to isolate a PHI area606. Once the selection tool 700 is confirmed on the diagnostic image600, the sanitizing engine 104 generates a preview of the sanitizeddiagnostic image for the user, such as by masking the area bounded bythe selection tool 700 with a blackout zone. In another embodiment, thearea bounded by the selection tool 700 can be deleted, blurred,obfuscated, cropped, or otherwise made illegible. In yet anotherembodiment, any pixels, characters, or text within the area bounded bythe selection tool 700 can be replaced with randomly generatedcharacters. In this embodiment, the sanitizing engine 104 utilizes analgorithm or script to generate the random characters such that therandom characters have no relation to the underlying patient, patientdata, medical data, or information that existed on the diagnostic imageprior to the de-identification process.

FIG. 7B is a view of a dialogue window with a selection tool used toselect non-PHI areas to create a de-identification profile, according toan embodiment of the invention. In an embodiment, instead of selectingPHI areas, user utilizes a selection tool 702 to select areas of thediagnostic image 600 that do not contain PHI, after the diagnostic imagehas undergone an OCR process, as described above. Referring to FIG. 7B,the selection tool 702 has been applied to various non-PHI areas,including non-PHI areas 604.

Once the selection tool 702 is confirmed on the diagnostic image 600,the sanitizing engine 104 generates a preview of the sanitizeddiagnostic image for the user, such as by masking any pixels,characters, or text not within the regions bounded by the selection tool700 with a blackout zone. In another embodiment, any pixels, characters,or text not within the regions bounded by the selection tool 702 aredeleted, blurred, obfuscated, cropped, or otherwise made illegible. Inyet another embodiment, any pixels, characters or text not within thearea bounded by the selection tool 702 are replaced with randomlygenerated characters. In this embodiment, the sanitizing engine 104utilizes an algorithm or script to generate the random characters suchthat the random characters have no relation to the underlying patient,patient data, medical data, or information that existed on thediagnostic image prior to the de-identification process.

FIG. 8 is a view of a region of interest identified by image analysis,according to an embodiment of the invention. In an embodiment, after thefirst stage of quality control is performed by the sanitizing engine104, a second stage of quality control is performed by the sanitizingengine 104 using an image analysis technique. the image analysis is usedto detect a gradient boundary 800 (i.e., a directional change in theintensity or color in an image) on the diagnostic image in order todetermine where the actual diagnostic portion 802 of the image ends. Thediagnostic portion 802 can be referred to the region of interest in thediagnostic image, and the gradient boundary 800 identifies the bounds ofthe region of interest.

Once the gradient boundary 800 is confirmed on the diagnostic image 600,the sanitizing engine 104 generates a preview of the sanitizeddiagnostic image for the user, such as by masking any pixels outside ofthe gradient boundary 800 a blackout zone. In another embodiment, anypixels outside of the gradient boundary 800 can be deleted, blurred,obfuscated, cropped, or otherwise made illegible. In yet anotherembodiment, any pixels, characters, or text outside of the gradientboundary 800 can be replaced with randomly generated characters. In thisembodiment, the sanitizing engine 104 utilizes an algorithm or script togenerate the random characters such that the random characters have norelation to the underlying patient, patient data, medical data, orinformation that existed on the diagnostic image prior to thede-identification process.

FIG. 9 is a table with exemplary DICOM metadata, according to anembodiment of the invention. The DICOM metadata, also referred to asDICOM tags, are DICOM data elements, or attributes, which are usually inthe format (XXXX,XXXX) with hexadecimal numbers, and which may bedivided further into DICOM group numbers (not shown) and DICOM elementnumbers (not shown). In addition, a DICOM value representation (VR) thatdescribes the data type and format of the attribute value can also beassociated with each DICOM tag (not shown).

In a preferred embodiment, the DICOM tags shown in FIG. 9 are utilizedfor the purposes of de-identification, however the tags shown in FIG. 9are exemplary, and the invention is not limited to these specific tagsbeing used for de-identification. For example, a user can configurespecific DICOM tags to be utilized for de-identification. In anembodiment, sanitization of the DICOM tags referred to in FIG. 9 arepreferred as they most comply with § 161.514(b)(2) and § 161.514(c) ofthe HIPAA Privacy Rule.

FIG. 10 is a flowchart illustrating the steps of re-identifying medicaldata, according to an embodiment of the invention. At step 1000, theuser selects a de-identified medical data to re-identify. In anembodiment, the user can be any entity or individual that has beengranted the ability to re-identify de-identified medical data, either bythe institution 106, the data provider 100, the recipient 112.

In an embodiment, re-identification may only be permitted if informedconsent has been provided by the patient. In another embodiment,re-identification requires an additional payment or surcharge. In yetanother embodiment, re-identified medical data may include securityfeatures such that it cannot be transmitted externally, printed,screenshot, or otherwise modified, shared, or disseminated.

At step 1002, the unique identification string, such as the SOP instanceUID, associated with the selected medical data at step 314 describedabove is retrieved. The unique identification string is compared tomedical records stored in the database 114.

At step 1004, the data entry corresponding to the unique identificationstring is identified in the database 114, and the header data and/orparseable document is retrieved using the unique identification stringas a key. Once the header data and/or parseable document is retrieved,the de-identified medical data is re-identified using the informationlocated in the header data and/or parseable document.

In an embodiment, if the medical data was purchased or obtained by theuser via the medical data marketplace 118, then the medical data may notbe eligible for re-identification.

While the principles of the disclosure have been illustrated in relationto the exemplary embodiments shown herein, the principles of thedisclosure are not limited thereto and include any modification,variation or permutation thereof.

The invention claimed is:
 1. A system for providing a medical datamarketplace, the system comprising: a database storing a plurality ofde-identified medical data sets, wherein each de-identified medical dataset is owned by a different data owner; a server coupled to thedatabase; and a computer-readable storage medium operably connected to aprocessor coupled to the server, the computer-readable storage mediumcontaining programming instructions that, when executed, cause theprocessor to: generate an interface that allows a customer to submit asearch request that includes at least one criteria, receive the searchrequest from the interface, query the database using the criteria toretrieve at least one matching medical data set from the plurality ofde-identified medical data sets, display the at least one matchingmedical data set on the interface, and facilitate a financialtransaction related to the at least one matching medical data setbetween a respective data owner and the customer, wherein the criteriais selected from a group consisting of a modality type, an equipmentmanufacturer, a body part, a study description, a protocol name, arequested procedure description, a scheduled procedure step description,and a keyword.
 2. The system of claim 1, wherein the criteria isselected from a group consisting of a patient race, a patient age, and apatient sex.
 3. The system of claim 1, wherein the criteria is a studydate or a study date range.
 4. The system of claim 1, wherein thecriteria is a geographic criteria or a demographic criteria.
 5. Thesystem of claim 1, wherein the financial transaction is a sale of the atleast one matching medical data set.
 6. The system of claim 1, whereinthe financial transaction is a license to the at least one matchingmedical data set.
 7. The system of claim 1, wherein the server and therespective data owner share proceeds from the financial transaction. 8.The system of claim 1, wherein the server receives a membership fee fromthe customer.
 9. The system of claim 1, wherein each of the plurality ofmedical data sets include a medical report and at least one diagnosticimage.
 10. A system for providing a medical data marketplace, the systemcomprising: a database storing a plurality of diagnostic image sets,wherein each diagnostic image set is owned by a different data owner; aserver coupled to the database; and a computer-readable storage mediumoperably connected to a processor coupled to the server, thecomputer-readable storage medium containing programming instructionsthat, when executed, cause the processor to: perform a de-identificationprocess on each of the plurality of diagnostic image sets to generate aplurality of de-identified diagnostic image sets, generate an interfacethat allows a customer to submit a search request that includes at leastone criteria, receive the search request from the interface, query thedatabase using the criteria to retrieve at least one matching diagnosticimage set from the plurality of de-identified diagnostic image sets,display the at least one matching diagnostic image set on the interface,and facilitate a financial transaction related to the at least onematching diagnostic image set between a respective data owner and thecustomer, wherein the criteria is selected from a group consisting of amodality type, an equipment manufacturer, a body part, a studydescription, a protocol name, a requested procedure description, ascheduled procedure step description, and a keyword.
 11. The system ofclaim 10, wherein the criteria is selected from a group consisting of apatient race, a patient age, and a patient sex.
 12. The system of claim10, wherein the criteria is a study date or a study date range.
 13. Thesystem of claim 10, wherein the criteria is a geographic criteria or ademographic criteria.
 14. The system of claim 10, wherein the financialtransaction is a sale of the at least one matching diagnostic image set.15. The system of claim 10, wherein the financial transaction is alicensing of the at least one matching diagnostic image set.
 16. Thesystem of claim 10, wherein the server receives a listing fee from eachof the different data owners.
 17. The system of claim 10, wherein atleast one of the server and the respective data owner share proceedsfrom the financial transaction.
 18. A system for providing a medicaldata marketplace, the system comprising: a database storing a pluralityof medical data sets, wherein each medical data set is owned by adifferent data owner; a server coupled to the database; and acomputer-readable storage medium operably connected to a processorcoupled to the server, the computer-readable storage medium containingprogramming instructions that, when executed, cause the processor to:perform a de-identification process on each of the plurality of medicaldata sets to generate a plurality of de-identified medical data sets,generate an interface that allows a customer to submit a search requestthat includes at least one criteria; receive the search request from theinterface, query the database using the criteria to retrieve at leastone matching medical data set from the plurality of de-identifiedmedical data sets, display the at least one matching medical data set onthe interface, and facilitate a financial transaction related to the atleast one matching medical data set between a respective data owner andthe customer, wherein the criteria is selected from a group consistingof a modality type, an equipment manufacturer, a body part, a studydescription, a protocol name, a requested procedure description, ascheduled procedure step description, and a keyword.
 19. The system ofclaim 18, wherein the de-identification process includes the steps of:retrieving, by the server, a medical image from a medical data set fromthe plurality of medical data sets; determining, by the server, amodality associated with the medical image; retrieving, by the server, ade-identification profile for the modality, wherein thede-identification profile specifies at least one area of the medicalimage that contains patient information; and applying, by a sanitizingengine coupled to the server, a blackout zone over the area of themedical image specified in the de-identification profile, wherein thepatient information within the blackout zone is deleted by thesanitizing engine.
 20. The system of claim 19, wherein thede-identification process further includes the steps of: detecting, bythe sanitizing engine, a boundary for a diagnostic portion of themedical image if no characters are detected in the area after theblackout zone has been applied; detecting, by the sanitizing engine, ifnon-black pixels are present outside of the boundary for the diagnosticportion; and performing a first operation by the sanitizing engine toconvert any non-black pixels detected outside of the boundary for thediagnostic portion to black pixels, or performing a second operation bythe sanitizing engine to encapsulate the medical image into a DICOMformat if non-black pixels are not detected outside of the boundary forthe diagnostic portion.